heike-starke documents

Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8
Documents Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8
First patient with trisomy 21 accompanied by an additional der(4)(:p11 → q11:) plus partial uniparental disomy 4p15-16
Documents First patient with trisomy 21 accompanied by an additional der(4)(:p11 → q11:) plus partial uniparental disomy 4p15-16
Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative
Documents Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative
Maternal insertion of 18q11.2–q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB)
Documents Maternal insertion of 18q11.2–q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB)
First postnatal case of mosaic del(22)/r(22)
Documents First postnatal case of mosaic del(22)/r(22)